Disease: Basal ganglia calcification- idiopathic 2
- <em>MAP3K6</em> Mutations in a Neurovascular Disease Causing Stroke, Cognitive Impairment, and Tremor
- 2q37 as a susceptibility locus for idiopathic basal ganglia calcification (IBGC) in a large South Tyrolean family
- A Case of Schizophrenia Like Psychosis Due to Fahr's Disease
- A comorbid case of familial Idiopathic Basal Ganglia Calcification ("Fahr´s Disease") associated with post-polio syndrome
- A de novo nonsense PDGFB mutation causing idiopathic basal ganglia calcification with laryngeal dystonia
- A fatal Mycobacterium chelonae infection in an immunosuppressed patient with systemic lupus erythematosus and concomitant Fahr's syndrome
- A Japanese family with idiopathic basal ganglia calcification with novel SLC20A2 mutation presenting with late-onset hallucination and delusion
- A Novel <em>SLC20A2</em> Mutation Associated with Familial Idiopathic Basal Ganglia Calcification and Analysis of the Genotype-Phenotype Association in Chinese Patients
- Analysis of candidate genes at the IBGC1 locus associated with idiopathic basal ganglia calcification ("Fahr's disease")
- Analysis of Candidate Genes at the IBGC1 Locus Associated with Idiopathic Basal Ganglia Calcification ("Fahr" Disease')
- Analysis of gene expression pattern and neuroanatomical correlates for SLC20A2 (PiT-2) shows a molecular network with potential impact in idiopathic basal ganglia calcification ("Fahr's disease")
- Analysis of the CTAGE5 P521A variation with the risk of familial idiopathic basal ganglia calcification in an Iranian population
- Association between a novel mutation in SLC20A2 and familial idiopathic basal ganglia calcification
- Basal ganglia calcification and novel compound heterozygous mutations in the PANK2 gene in a Chinese boy with classic Pantothenate kinase-associated neurodegeneration: A case report
- Basal ganglia calcification: a Fahr's disease case report
- Bi-allelic JAM2 Variants Lead to Early-Onset Recessive Primary Familial Brain Calcification
- Bilateral basal ganglia calcification and recurrent generalized seizures as initial presentation of idiopathic hypoparathyroidism in an infant
- Bilateral basal ganglia calcifications and Graves' disease in a young patient: A very rare association (case report)
- Brain Calcification and Movement Disorders
- Canadian national hypoparathyroidism registry: an overview of hypoparathyroidism in Canada
- Characteristics and therapeutic potential of sodium-dependent phosphate cotransporters in relation to idiopathic basal ganglia calcification
- Chronic Hypoparathyroidism Due to Partial Thyroidectomy with Intracranial Calcification
- Clinical features of familial idiopathic basal ganglia calcification caused by a novel mutation in the SLC20A2 gene
- Cloning, genomic structure, and expression profiles of TULIP1 (GARNL1), a brain-expressed candidate gene for 14q13-linked neurological phenotypes, and its murine homologue
- Cognitive impairment and epilepsy seizure caused by hypoparathyroidism
- Disruption of a brain transcription factor, NPAS3, is associated with schizophrenia and learning disability
- Diverse genetic aetiologies and clinical outcomes of paediatric hypoparathyroidism
- Dysarthria: a case report
- Effect of basal ganglia calcification on its glucose metabolism and dopaminergic function in idiopathic hypoparathyroidism
- Evaluation of SLC20A2 mutations that cause idiopathic basal ganglia calcification in Japan
- Exclusion of linkage to chromosomes 14q, 2q37 and 8p21.1-q11.23 in a Serbian family with idiopathic basal ganglia calcification
- Expression of osteogenic molecules in the caudate nucleus and gray matter and their potential relevance for Basal Ganglia calcification in hypoparathyroidism
- Extensive intracranial calcifications in a patient with a novel polymerase γ-1 mutation
- Fahr disease: use of susceptibility-weighted imaging for diagnostic dilemma with magnetic resonance imaging
- Fahr syndrome associated to hypoparathyroidy, revealed by dermatologic manifestation
- Fahr's disease associated with anaplastic ependymoma: a case report and review of the literature
- Fahr's disease linked to a novel SLC20A2 gene mutation manifesting with dynamic aphasia
- Fahr's Disease Presenting with Aneurysmal Subarachnoid Hemorrhage
- Fahr's Disease With Intracerebral Hemorrhage at the Uncommon Location: A Case Report
- Fahr's syndrome due to hypoparathyroidism revisited: A case of parkinsonism and a review of all published cases
- Fahr's syndrome in Southern Tunisia: A broad spectrum of clinical and etiological features
- Familial idiopathic basal ganglia calcification (Fahr's disease) without neurological, cognitive and psychiatric symptoms is not linked to the IBGC1 locus on chromosome 14q
- Familial idiopathic basal ganglia calcification with a heterozygous missense variant (c.902C>T/p.P307L) in SLC20A2 showing widespread cerebrovascular lesions
- Familial idiopathic basal ganglia calcification: Histopathologic features of an autopsied patient with an SLC20A2 mutation
- Familial idiopathic hypoparathyroidism, sensorineural deafness and renal dysplasia
- Frontal-subcortical dementias
- Functional improvement in a patient with cerebral calcinosis using a bisphosphonate
- Genomic Diagnoses for Ectopic Intracerebral Calcifications
- High Levels of Copper, Zinc, Iron and Magnesium, but not Calcium, in the Cerebrospinal Fluid of Patients with Fahr's Disease
- Human induced pluripotent stem cells generated from a patient with idiopathic basal ganglia calcification
- Hypoparathyroidism and early onset dementia: Fahr syndrome should be suspected
- Idiopathic basal ganglia calcification and pathological hoarding
- Idiopathic basal ganglia calcification presenting as schizophrenia-like psychosis and obsessive-compulsive symptoms: A case report
- Idiopathic basal ganglia calcifications: an atypical presentation of PKAN
- Idiopathic bilateral basal ganglia calcification (Fahr's disease) presenting with psychotic depression and criminal violence: a case report with forensic aspect
- Idiopathic brain calcification in a patient with hereditary hemochromatosis
- Idiopathic Fahr's disease
- Idiopathic hypoparathyroidism and adhesive capsulitis of the shoulder in two first-degree relatives
- Idiopathic hypoparathyroidism presenting with severe hypocalcemia and asymptomatic basal ganglia calcification followed by acute intracerebral bleed
- Idiopathic hypoparathyroidism with extensive intracranial calcification in children: First report from Saudi Arabia
- Infantile convulsions and paroxysmal kinesigenic choreoathetosis in a patient with idiopathic hypoparathyroidism
- Inherited Arterial Calcification Syndromes: Etiologies and Treatment Concepts
- Inorganic phosphorus (Pi) in CSF is a biomarker for SLC20A2-associated idiopathic basal ganglia calcification (IBGC1)
- Late diagnosis and atypical brain imaging of Aicardi-Goutières syndrome: are we failing to diagnose Aicardi-Goutières syndrome-2?
- Living with idiopathic basal ganglia calcification 3: a qualitative study describing the lives and illness of people diagnosed with a rare neurological disease
- Localization of type-III sodium-dependent phosphate transporter 2 in the mouse brain
- Loss of function of Slc20a2 associated with familial idiopathic Basal Ganglia calcification in humans causes brain calcifications in mice
- Mineralizing angiopathy presenting with recurrence of basal ganglia stroke following minor head trauma
- Mutation of the PDGFRB gene as a cause of idiopathic basal ganglia calcification
- Mutation screening of PDGFB gene in Chinese population with primary familial brain calcification
- Mutations in SLC20A2 link familial idiopathic basal ganglia calcification with phosphate homeostasis
- Neuroprotective effect of 5-aminolevulinic acid against low inorganic phosphate in neuroblastoma SH-SY5Y cells
- Neuropsychiatric symptoms revealing pseudohypoparathyroidism with Fahr's syndrome
- Neuroradiologic evidence of pre-synaptic and post-synaptic nigrostriatal dopaminergic dysfunction in idiopathic Basal Ganglia calcification: a case report
- Novel SLC20A2 mutations identified in southern Chinese patients with idiopathic basal ganglia calcification
- Parathyroid hormone gene polymorphism and sporadic idiopathic hypoparathyroidism
- Partial reduced Pi transport function of PiT-2 might not be sufficient to induce brain calcification of idiopathic basal ganglia calcification
- PDGF-BB is involved in phosphate regulation via the phosphate transporters in human neuroblastoma SH-SY5Y cells
- PDGFB partial deletion: a new, rare mechanism causing brain calcification with leukoencephalopathy
- Pediatric Idiopathic Basal Ganglia Calcification and Spherocytosis With Chromosome 8p11 Deletion
- Population and computational analysis of the MGEA6 P521A variation as a risk factor for familial idiopathic basal ganglia calcification (Fahr's disease)
- Presence of spondyloarthropathy and its clinical profile in patients with hypoparathyroidism
- Prevalence and clinical significance of computerized tomography verified idiopathic calcinosis of the basal ganglia
- Prevalence and progression of basal ganglia calcification and its pathogenic mechanism in patients with idiopathic hypoparathyroidism
- Primary familial brain calcification in the 'IBGC2' kindred: All linkage roads lead to SLC20A2
- Progressive idiopathic bilateral striato-pallido-dentate calcinosis (Fahr's disease) in a person with anabolic steroid abuse
- PSEUDOPSEUDOHYPOPARATHYROIDISM AS A CAUSE OF FAHR SYNDROME: HYPOPARATHYROIDISM NOT THE ONLY ONE
- Recurrent convulsions, hypocalcemia, and hypoparathyroidism related to delayed diagnosis of 22q11.2 deletion syndrome in a middle-aged man
- Role of phosphate transporter PiT-2 in the pathogenesis of primary brain calcification
- Schizophrenia in DiGeorge Syndrome: A Unique Case Report
- Seizures as the first manifestation of chromosome 22q11.2 deletion syndrome in a 40-year old man: a case report
- Serum Fetuin-A Levels in Patients with Bilateral Basal Ganglia Calcification
- SLC20A2 variants cause dysfunctional phosphate transport activity in endothelial cells induced from Idiopathic Basal Ganglia Calcification patients-derived iPSCs
- SLC20A2-Associated Idiopathic Basal Ganglia Calcification-Related Recurrent Psychosis Response to Low-Dose Antipsychotics: A Case Report and Literature Review
- Spectrum of neurological manifestations of idiopathic hypoparathyroidism and pseudohypoparathyroidism
- The causative gene of Parkinsonism and its medical treatment strategy
- The first Japanese case of primary familial brain calcification caused by an MYORG variant
- The Impact of COVID-19 Infection on a Neurologically Compromised Male With Fahr's Disease Presenting With Acute Delirium and Aspiration Pneumonia: A Case Report
- The type III transporters (PiT-1 and PiT-2) are the major sodium-dependent phosphate transporters in the mice and human brains
- White matter involvement in a family with a novel PDGFB mutation